Ex) Article Title, Author, Keywords
Online ISSN 2288-5978
Ex) Article Title, Author, Keywords
Journal of the Korean Society of Food Science and Nutrition 2016; 45(11): 1604-1609
Published online November 30, 2016
Copyright © The Korean Society of Food Science and Nutrition.
Jin Gwan Kwon1, Changon Seo1, Seong Su Hong1, Dong-Wan Seo2, Joa Sub Oh2, and Jin Kyu Kim1
1Gyeonggi Institute of Science & Technology Promotion; 2College of Pharmacy, Dankook University
An HPLC analysis method was developed for standard determination of marmesin as a functional health material in Broussonetia kazinoki extract. HPLC was performed on a C18 Kromasil column (4.6×250 mm, 5 μm) with a gradient elution of 0.1% (v/v) trifluoroacetic acid and acetonitrile at a flow rate of 1.0 mL/min at 30°C. The analyte was detected at 330 nm. The HPLC method was validated in accordance with International Conference on Harmonization guidelines for analytical procedures with respect to specificity, precision, accuracy, and linearity. The limit of detection and quantitation were 6.2 and 18.6 μg/mL, respectively. Calibration curves showed good linearity (r2>0.9999), and the precision of analysis was satisfactory (less than 0.3%). Recoveries of quantified compound ranged from 100.35 to 101.18%. This result indicates that the established HPLC method is very useful for the determination of marker compounds in B. kazinoki extracts.
Keywords: Broussonetia kazinoki, marmesin, validation, HPLC, functional health food
Journal of the Korean Society of Food Science and Nutrition 2016; 45(11): 1604-1609
Published online November 30, 2016
Copyright © The Korean Society of Food Science and Nutrition.
Jin Gwan Kwon*1, Changon Seo*1, Seong Su Hong*1, Dong-Wan Seo*2, Joa Sub Oh*2, and Jin Kyu Kim*1
*1Gyeonggi Institute of Science & Technology Promotion; *2College of Pharmacy, Dankook University
An HPLC analysis method was developed for standard determination of marmesin as a functional health material in Broussonetia kazinoki extract. HPLC was performed on a C18 Kromasil column (4.6×250 mm, 5 μm) with a gradient elution of 0.1% (v/v) trifluoroacetic acid and acetonitrile at a flow rate of 1.0 mL/min at 30°C. The analyte was detected at 330 nm. The HPLC method was validated in accordance with International Conference on Harmonization guidelines for analytical procedures with respect to specificity, precision, accuracy, and linearity. The limit of detection and quantitation were 6.2 and 18.6 μg/mL, respectively. Calibration curves showed good linearity (r2>0.9999), and the precision of analysis was satisfactory (less than 0.3%). Recoveries of quantified compound ranged from 100.35 to 101.18%. This result indicates that the established HPLC method is very useful for the determination of marker compounds in B. kazinoki extracts.
Keywords: Broussonetia kazinoki, marmesin, validation, HPLC, functional health food
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